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The Regulatory Affairs team at Day One Biopharmaceuticals plays a critical role in ensuring that the company’s cancer therapies comply with all regulatory requirements throughout their development. This team is responsible for managing regulatory submissions, maintaining quality standards, and overseeing compliance with Good Clinical Practice (GCP), while facilitating communication with regulatory agencies to secure necessary approvals for clinical trials and product launches. Their expertise is essential in navigating complex regulations, ensuring the safety and efficacy of new therapies for patients of all ages.